Phase 2
N=120
A Study to Evaluate Safety and Immunogenicity of One and Two Doses of IMVAMUNE® Smallpox Vaccine in 56-80 Year Old Vaccinia-experienced Subjects
Smallpox
Bottom Line
View on ClinicalTrials.gov: NCT00857493 ↗Enrolled (actual)
120
Serious AEs
3.3%
Results posted
Jan 2019
Primary outcome: Primary: Related Serious Adverse Events — 0; 0 Participants
Study Design & Population
- Study type
- Interventional
- Phase
- Phase 2
- Interventions
- IMVAMUNE (Biological)
- Age
- Adult, Older Adult · 56+ yrs
- Sex
- All
- Sponsor
- Bavarian Nordic
- Primary completion
- Aug 2010
Outcome Measures
| Outcome | Result | p-value |
|---|---|---|
| PRIMARY Related Serious Adverse Events |
0; 0 | — |
| SECONDARY Unsolicited Non-serious AEs: Intensity |
73; 58; 60; 50; 9; 7 | — |
| SECONDARY Unsolicited Non-serious AEs: Relationship to Vaccination |
32; 26; 6; 2; 20; 13 | — |
| SECONDARY Related Grade >=3 Adverse Events |
3; 1 | — |
| SECONDARY Cardiac Signs or Symptoms |
5; 0; 0; 0; 0; 0 | — |
| SECONDARY Solicited Local Adverse Events |
46; 36; 4; 1; 49; 37 | — |
| SECONDARY Solicited General Adverse Events |
2; 1; 2; 0; 0; 0 | — |
| SECONDARY ELISA Response Rate |
98.4; 19.0; 96.6; 19.0; 98.3; 96.6 | — |
| SECONDARY ELISA Seroconversion Rate |
83.6; 1.7; 79.7; 3.4; 83.3; 82.8 | — |
| SECONDARY ELISA GMT |
129.0; 105.3; 622.5; 98.5; 501.2; 101.0 | — |
| SECONDARY PRNT Response Rate |
83.6; 15.5; 81.4; 10.3; 96.7; 82.8 | — |
| SECONDARY PRNT Seroconversion Rate |
73.8; 10.3; 71.2; 8.6; 90.0; 77.6 | — |
| SECONDARY PRNT GMT |
11.9; 11.3; 111.4; 9.2; 79.5; 11.3 | — |
| SECONDARY Correlation PRNT vs ELISA Titers |
0.704; 0.489; 0.569; 0.492; 0.660; 0.697 | — |
Summary
A Randomized, Double-Blind, Placebo-Controlled Phase II Study to Evaluate Safety and Immunogenicity of One and Two Doses of IMVAMUNE® Smallpox Vaccine in 56-80 Year Old Vaccinia-Experienced Subjects
Eligibility Criteria
Inclusion Criteria
- Male and female subjects 56-70 years of age. If no safety concerns are identified upon review of the safety data from the first 30 subjects enrolled, the age range is extended up to 80 years.
- Time since most current smallpox vaccination > 10 years.
- The subject has read, signed and dated the Informed Consent Form (ICF), successfully completed (at least 90% correct [no more than 3 attempts allowed]) the test of understanding and has signed the Health Insurance Portability and Accountability Act (HIPAA) authorization form.
- Women must have a negative serum pregnancy test at screening and negative urine pregnancy test within 24 hours prior to vaccination.
- Women of childbearing potential (WOCBP) must have used an acceptable method of contraception for 30 days prior to the first vaccination, must agree to use an acceptable method of contraception during the study and must not plan to become pregnant for at least 28 days after the last vaccination. (Acceptable contraception methods are restricted to abstinence, barrier contraceptives, intrauterine contraceptive devices or licensed hormonal products).
- Weight: ≥ 100 pounds (45.5 kg) and ≤ 330 pounds (150 kg).
- White blood cells ≥ 2500/mm3 and 14 days) of systemic, i.e. parenteral or oral, corticosteroids (> 5 mg prednisone [or equivalent] per day), radiation or immune-modifying drugs.
- Periodic steroid injections, e.g. intraarticular, are not allowed within 30 days prior to the first vaccination and throughout the study until Visit 5 (V5).
- Post organ transplant subjects whether or not receiving chronic immunosuppressive therapy.
- Uncontrolled serious infection, i.e. not responding to antimicrobial therapy.
- History of any serious medical condition, which in the opinion of the investigator would compromise the safety of the subject or prevent the subject from complying with study requirements.
- History of or active autoimmune disease, e.g. Type I diabetes. Persons with vitiligo or thyroid disease taking thyroid hormone replacement are not excluded.
- Skin cancer in the past six months. If treatment for skin cancer was successfully completed more than six months ago and the malignancy is considered to be cured, the subject may be enrolled. Subjects with history of skin cancer must not be vaccinated at the previous site of cancer.
- Any other malignancy in the past five years. If treatment for cancer was successfully completed more than 5 years ago and the malignancy is considered to be cured, the subject may be enrolled.
- Clinically significant hematological, renal, hepatic, pulmonary, central nervous, cardiovascular or gastrointestinal disorders which are not adequately controlled by medical treatment within the last 12 weeks before vaccination as judged by the site's Principal Investigator.
- History of myocardial infarction, congestive heart failure with marked limitation of activity due to symptoms, e.g. walking short distances [20 100 m] (i.e. > Grade II according to the New York Heart Association), cardiomyopathy and stroke or transient ischemic attack in the past two years.
- Uncontrolled high blood pressure defined as systolic blood pressure ≥ 150 mm Hg and/or ≥ diastolic blood pressure ≥ 100 mm Hg within the last six months.
- Subjects with active coronary heart disease manifested by angina, even if on medication.
- 25 % or greater risk of developing a myocardial infarction or coronary death within the next 10 years using the National Cholesterol Education Program's Risk Assessment Tool: http://hin.nhlbi.nih.gov/atpiii/calculator.asp
- Clinically significant mental disorder not adequately controlled by medical treatment.
- History of chronic alcohol abuse (40 g/day, e.g. 3 glasses of beer or 2 glasses of wine for at least six months) and/or intravenous drug abuse (within the last six months). Subjects with a history of other substance and/or alcohol abuse are also excluded if - in the opinion of the investigator - the abuse could prevent t
Data sourced from ClinicalTrials.gov (NCT00857493). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.